Manager, Solutions
2 weeks ago
Vantive: A New Company Built On Our Legacy
Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.
At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.
*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.
Essential Duties and Responsibilities:
Functional management of team – Hiring, competency building, training, setting SMART goals, ACE Check-ins, providing regular feedback, performance management, development planning, career coaching, budget planning & tracking. Responsible for handling team working closely with PDO Organization, Project Management, Regulatory, Quality and the other cross-functions on Renal Care Projects related to product design change and new product registration in compliance with current international/regional/national regulations. Responsible for identifying necessary resources and building appropriate teams in to support product development and lifecycle management. Expected to develop, document, test and manage product related changes in accordance with established Renal Care product processes and stay in alignment with QMS. Responsible for identifying outsourcing partners for product development and lifecycle management related activities as necessary. Develop culture of innovation Responsible for identifying areas for product enhancements. Establish culture within team to create, maintain and update technical & design documentation according to Good Documentation Practices.Qualifications:
Masters / PhD Degree in Science or Pharmaceutical disciplines is required. Must be able to interact on a technical level.Education and/or Experience:
MS in Chemistry, MPharm in Pharmacy, Development Engineer or equivalent with 13-17 years of relevant experience or PhD with 9+ years of relevant experience in medical device and/or drug R&D. Good knowledge of Renal HD therapies and products Good knowledge of product development stages and life cycle management: development, stability, clinical, registration, process transfer, production, suppliers, customer service etc. Good knowledge of Design Control documentation and process. Working knowledge of international/regional/national regulations and standards. Portfolio management and business acumen of HD products. Experience with people management and building high performing teams. Proven coaching and mentoring skills with ability to motivate, inspire and get the best out of team. Excellent oral and written communication skills Strong analytical and problem-solving skills Good organizational skills. Ability to effectively organize and prioritize tasks. Demonstrated abilities to provide technical and functional leadership to the team on product lifecycle management related projects/activities. Must be able to able to carry out strategy and vision set by upper management and be able to communicate the vision to team.-
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